The choice for the optimal therapy in advanced biliary tract cancers: Chemotherapy, targeted therapies or immunotherapy
- PMID: 32109491
- DOI: 10.1016/j.pharmthera.2020.107517
The choice for the optimal therapy in advanced biliary tract cancers: Chemotherapy, targeted therapies or immunotherapy
Abstract
Biliary tract cancers (BTCs) represent a heterogeneous group that includes intrahepatic cholangiocarcinomas (CCAs), perihilar-CCAs or Klatskin tumors, extrahepatic-CCAs, and gallbladder adenocarcinoma. These entities have distinct demographics, risk factors, clinical presentation, and molecular characteristics. In advanced BTCs, the recommendations are mainly supporting a doublet chemotherapy regimen using cisplatin/gemcitabine (CisGem) with a 5-year overall survival rate close to 5% and median overall survival (mOS) of less than a year. The lack of overall efficacy stresses the need for personalized therapies. Recently, whole-genome and transcriptome sequencing highlighted the diversity of BTCs' subtypes. Distinct genetic alterations were retrieved according to the localization, with a high rate of potentially actionable alterations. Targeted therapies and immunotherapy have since then been tested for BTCs, trying to propose a more personalized treatment. This review describes the different therapeutic options, validated and in development, for patients with advanced BTCs.
Keywords: Biliary tract cancers; Cholangiocarcinoma; Genome sequencing; Immunotherapy; Targeted therapy.
Copyright © 2020 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of Competing Interest Dr. Palmieri and Dr. Lavole received honoraria from Servier outside the submitted work. Pr. Coriat received honoraria from AAA, Ipsen, Novartis, Merck, Amgen, Roche, Pfizer, Biologyx and Bayer outside the submitted work. The remaining authors disclose no conflicts. We wish to confirm that there has been no significant financial support for this work that could have influenced its outcome.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
